Composition for sealing material film and sealing material film containing the same
A composition with a specific organic peroxide crosslinking agent and crosslinking aid enhances the affinity and crosslinking efficiency of ethylene/α-olefin copolymers, addressing prolonged impregnation times and improving productivity in encapsulant film production for solar cell modules.
Patent Information
- Application Number
- JP2024553490
- Authority / Receiving Office
- JP · JP
- Patent Type
- Applications
- Current Assignee / Owner
- Priority Date
- 2022-08-26
- Filing Date
- 2023-05-31
- Publication Date
- 2025-09-04
AI Technical Summary
The production of encapsulant films for solar cell modules is hindered by the low affinity between crosslinking agents and ethylene/α-olefin copolymers, leading to prolonged impregnation times and reduced productivity.
A composition for encapsulant films comprising an ethylene/α-olefin copolymer, an organic peroxide crosslinking agent with a one-hour half-life temperature of 115 to 130°C, a crosslinking aid with a specific chemical structure, and a silane coupling agent, which enhances the affinity and crosslinking efficiency.
The composition significantly shortens impregnation time and improves crosslinking, enhancing the economic efficiency and durability of the encapsulant film production process.
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Abstract
Description
[Technical Field]
[0001] This application claims the benefit of priority based on Korean Patent Application No. 2022-0107467, filed on August 26, 2022, and all contents disclosed in the documents of this Korean patent application are incorporated herein by reference.
[0002] The present invention relates to a composition for an encapsulant film containing an ethylene / α-olefin copolymer, an encapsulant film, and a solar cell module. [Background technology]
[0003] As global environmental and energy issues become increasingly serious, solar cells are attracting attention as a means of generating energy without the risk of environmental pollution or depletion. When solar cells are used outdoors, such as on the roof of a building, they are generally used in the form of a solar cell module. When manufacturing a solar cell module, to obtain a crystalline solar cell module, the following layers are laminated in this order: front glass / solar cell encapsulant / crystalline solar cell element / solar cell encapsulant / rear glass (or rear protective sheet). The solar cell encapsulant is generally made of an ethylene / vinyl acetate copolymer or an ethylene / α-olefin copolymer, which have excellent transparency, flexibility, adhesiveness, etc.
[0004] A solar cell module is a package in which solar cell elements such as silicon, gallium-arsenide, or copper-indium-selenium are protected with an upper transparent protective material and a lower substrate protective material, and the solar cell elements and protective material are fixed in place with a sealant. Generally, the sealant for the solar cell elements in a solar cell module is made by extruding an ethylene / α-olefin copolymer containing an organic peroxide or a silane coupling agent into a sheet, and the solar cell elements are sealed using the resulting sheet sealant to produce a solar cell module.
[0005] In order to improve productivity during the production of the above-mentioned solar cell module, one possible solution is to increase the affinity between various raw materials contained in the encapsulant film composition and the ethylene / α-olefin copolymer to enhance water absorption. In particular, crosslinking agents and crosslinking aids, which are essential for the production of encapsulant films, are polar substances and have low water absorption properties for non-polar ethylene / α-olefin copolymers, which is considered to be one of the factors that cause reduced productivity. [Prior art documents] [Patent documents]
[0006] [Patent Document 1] Japanese Patent Application Laid-Open No. 2015-211189 Summary of the Invention [Problem to be solved by the invention]
[0007] An object of the present invention is to shorten the impregnation time of an ethylene / α-olefin copolymer in the initial step during the production of an encapsulant film by using a crosslinking agent, crosslinking aid, etc. that have high affinity with the ethylene / α-olefin copolymer. [Means for solving the problem]
[0008] In order to solve the above problems, the present invention provides a composition for an encapsulant film, an encapsulant film, and a solar cell module.
[0009] (1) The present invention provides a composition for an encapsulant film, comprising an ethylene / α-olefin copolymer, an organic peroxide crosslinking agent, a crosslinking aid, and a silane coupling agent, wherein the crosslinking aid comprises a compound represented by the following chemical formula 1, and the organic peroxide crosslinking agent has a one-hour half-life temperature of 115 to 130°C:
[0010] [ka]
[0011] In the above Chemical Formula 1, n is an integer of 2 to 6.
[0012] (2) The present invention provides the composition for an encapsulant film according to (1) above, wherein the organic peroxide crosslinking agent is at least one selected from the group consisting of t-butylperoxy 2-ethylhexyl carbonate, t-amylperoxy 2-ethylhexyl carbonate, 1,1-di(t-butylperoxy)-3,3,5-trimethylcyclohexane, 1,1-di(t-butylperoxy)-cyclohexane, 2,2-di(t-amylperoxy)-butane, 2,2-di(t-butylperoxy)-butane, n-butyl-4,4-di(t-butylperoxy)valerate, polyether poly(t-butylperoxycarbonate), t-amylperoxy 3,5,5-trimethylhexanoate, t-butylperoxyacetate, and t-butylperoxybenzoate.
[0013] (3) The present invention provides the composition for a sealing material film according to (1) or (2) above, wherein the organic peroxide crosslinking agent is contained in an amount of 0.1 to 3.0 parts by weight based on 100 parts by weight of the ethylene / α-olefin copolymer.
[0014] (4) The present invention provides the composition for an encapsulating material film according to any one of (1) to (3), wherein the crosslinking aid is present in an amount of 0.1 to 3.0 parts by weight based on 100 parts by weight of the ethylene / α-olefin copolymer.
[0015] (5) The present invention provides the composition for an encapsulant film according to any one of (1) to (4), wherein the silane coupling agent is contained in an amount of 0.1 to 1.0 parts by weight based on 100 parts by weight of the ethylene / α-olefin copolymer.
[0016] (6) The present invention provides the composition for an encapsulant film according to any one of (1) to (5) above, wherein the crosslinking aid further contains an allyl group-containing compound.
[0017] (7) The present invention provides the composition for an encapsulant film according to (6) above, wherein the allyl group-containing compound includes at least one compound selected from the group consisting of triallyl isocyanurate, triallyl cyanurate, diallyl phthalate, diallyl fumarate, and diallyl maleate.
[0018] (8) The present invention provides the composition for a sealing material film according to (6) and (7) above, wherein the molar ratio of the compound represented by Chemical Formula 1 to the allyl group-containing compound is 1:0.1 to 1:10.
[0019] (9) The present invention provides the composition for an encapsulant film according to any one of (1) to (8), wherein the α-olefin comprises one or more selected from the group consisting of propylene, 1-butene, 1-pentene, 4-methyl-1-pentene, 1-hexene, 1-heptene, 1-octene, 1-decene, 1-undecene, 1-dodecene, 1-tetradecene, 1-hexadecene, and 1-eicosene.
[0020] (10) The present invention provides the composition for an encapsulant film according to any one of (1) to (9), wherein the α-olefin is contained in an amount of more than 0 and not more than 99 mol% based on the ethylene / α-olefin copolymer.
[0021] (11) The present invention provides an encapsulant film comprising the composition for an encapsulant film according to any one of (1) to (10) above.
[0022] (12) The present invention provides a solar cell module including the encapsulant film according to (11) above. [Effects of the Invention]
[0023] When a sealant film is produced using the composition for sealant films according to the present invention, the impregnation time of the ethylene / α-olefin copolymer can be shortened, thereby improving the economic efficiency of the sealant film production process. In addition, the composition for sealant films produced using the present invention exhibits an excellent degree of crosslinking. DETAILED DESCRIPTION OF THE INVENTION
[0024] The present invention will now be described in more detail so that the present invention may be more easily understood.
[0025] The terms and words used in the description of the present invention and the claims should not be interpreted in a limited way to their ordinary or dictionary meanings, but should be interpreted in a way that is consistent with the technical idea of the present invention, based on the principle that the inventors can appropriately define the concepts of terms in order to best describe their invention.
[0026] <Composition for sealing film> The composition for an encapsulant film of the present invention comprises (a) an ethylene / α-olefin copolymer, (b) an organic peroxide crosslinking agent, (c) a crosslinking aid, and (d) a silane coupling agent, and the crosslinking aid comprises a compound represented by the following chemical formula 1:
[0027] Each component will be described in detail below.
[0028] (a) Ethylene / α-olefin copolymer The composition for an encapsulant film of the present invention includes an ethylene / α-olefin copolymer, which is produced by copolymerizing ethylene with an α-olefin monomer, and the α-olefin, which refers to the portion of the copolymer derived from the α-olefin monomer, is an α-olefin having 4 to 20 carbon atoms, specifically propylene, 1-butene, 1-pentene, 4-methyl-1-pentene, 1-hexene, 1-heptene, 1-octene, 1-decene, 1-undecene, 1-dodecene, 1-tetradecene, 1-hexadecene, or 1-eicosene, and may be used alone or in combination of two or more thereof.
[0029] Among them, the α-olefin may be 1-butene, 1-hexene, or 1-octene, and preferably 1-butene, 1-octene, or a combination thereof.
[0030] In addition, the content of the α-olefin in the ethylene / α-olefin copolymer may be appropriately selected within a range that satisfies the above physical property requirements, and specifically, it may be more than 0 and not more than 99 mol%, or 10 to 50 mol%, but is not limited thereto.
[0031] In the present invention, the method for preparing or route for obtaining the ethylene / α-olefin copolymer is not limited, and a person skilled in the art can select and use a suitable one in consideration of the physical properties and purpose of the composition for the encapsulant film.
[0032] (b) Organic peroxide crosslinking agent The encapsulant film composition of the present invention contains an organic peroxide crosslinking agent. The organic peroxide crosslinking agent can act as a radical initiator in the preparation step of a silane-modified resin composition to initiate a reaction in which an unsaturated silane compound is grafted onto the resin composition. Furthermore, during the lamination step in the manufacture of an optoelectronic device, the organic peroxide crosslinking agent forms crosslinks between the silane-modified resin compositions or between the silane-modified resin composition and an unmodified resin composition, thereby improving the heat resistance and durability of the final product, for example, the encapsulant sheet.
[0033] In particular, the solar cell encapsulant may contain an organic peroxide as a crosslinking agent, and the organic peroxide plays a role in improving the weather resistance of the solar cell encapsulant.
[0034] The organic peroxide crosslinking agent may have a one-hour half-life temperature of 115 to 130°C.
[0035] The "one-hour half-life temperature" refers to the temperature at which the half-life of the crosslinking agent is one hour. The temperature at which a radical initiation reaction efficiently occurs varies depending on the one-hour half-life temperature. Therefore, when an organic peroxide crosslinking agent having a one-hour half-life temperature within the above range is used, the radical initiation reaction, i.e., the crosslinking reaction, can proceed effectively at the temperature of a lamination process for manufacturing an optoelectronic device.
[0036] Specifically, the organic peroxide crosslinking agent may be one or more selected from the group consisting of t-butylperoxy 2-ethylhexyl carbonate (TBEC), t-amylperoxy 2-ethylhexyl carbonate (TAEC), 1,1-di(t-butylperoxy)-3,3,5-trimethylcyclohexane, 1,1-di(t-butylperoxy)-cyclohexane, 2,2-di(t-amylperoxy)-butane, 2,2-di(t-butylperoxy)-butane, n-butyl-4,4-di(t-butylperoxy)valerate, polyether poly(t-butylperoxycarbonate), t-amylperoxy 3,5,5-trimethylhexanoate, t-butylperoxyacetate, and t-butylperoxybenzoate, but is not limited thereto.
[0037] When the 1-hour half-life temperature of the organic peroxide crosslinking agent is within the above range, the radical decomposition rate of the crosslinking agent is not faster than the crosslinking rate of the ethylene / α-olefin copolymer during the crosslinking process, thereby achieving the desired degree of crosslinking. Furthermore, under normal crosslinking conditions (140 to 150°C), the slow radical decomposition rate of the crosslinking agent can be prevented from slowing down the crosslinking rate.
[0038] The organic peroxide crosslinking agent may be contained in an amount of 0.1 to 3.0 parts by weight, 0.1 to 2.0 parts by weight, or 0.5 to 1.5 parts by weight, based on 100 parts by weight of the ethylene / α-olefin copolymer. When the organic peroxide crosslinking agent is contained in the above range, the effect of improving heat resistance is sufficiently exhibited, and the formability of the encapsulant film is excellent, so that process restrictions and deterioration of the physical properties of the encapsulant do not occur.
[0039] (c) Crosslinking aid The composition for an encapsulant film of the present invention contains a crosslinking aid, and the crosslinking aid contains a compound represented by the following Chemical Formula 1.
[0040] [ka]
[0041] In the above Chemical Formula 1, n is an integer of 2 to 6.
[0042] Specifically, the compound represented by Chemical Formula 1 may be selected from the following compounds:
[0043] [ka]
[0044] [ka]
[0045] The crosslinking coagent used in the present invention is non-polar, unlike conventional crosslinking coagents such as triallyl isocyanurate, and has excellent affinity with the ethylene / α-olefin copolymer, allowing for rapid impregnation.
[0046] Furthermore, the cyclohexane and carboxylate functional groups located at the center of the cross-linking coagent structure firmly fix the polymer chains together, enabling an excellent degree of cross-linking to be achieved.
[0047] In this way, by including the crosslinking aid together with the organic peroxide crosslinking agent in the composition for a sealant film, the absorption rate of the crosslinking agent and the crosslinking aid into the composition for a sealant film is significantly improved, and the degree of crosslinking is further increased, thereby maintaining the heat resistance and durability of final products such as sealant films and significantly improving production economy.
[0048] In the present invention, the composition for an encapsulant film may further contain an allyl group-containing compound as a crosslinking aid.
[0049] The allyl group-containing compound may include one or more selected from the group consisting of triallyl isocyanurate, triallyl cyanurate, diallyl phthalate, diallyl fumarate, and diallyl maleate.
[0050] Here, the molar ratio of the compound represented by Chemical Formula 1 to the allyl group-containing compound may be 1:0.1 to 1:10, specifically 1:0.2 to 1:5, and more specifically 1:0.3 to 1:4.
[0051] When the content is within the above range, the impregnation time of the ethylene / α-olefin copolymer can be shortened and the degree of crosslinking of the composition for an encapsulant film can be increased.
[0052] The crosslinking aid may be contained in an amount of 0.1 to 3.0 parts by weight, specifically 0.1 to 2.0 parts by weight, or 0.25 to 1.50 parts by weight, based on 100 parts by weight of the ethylene / α-olefin copolymer.
[0053] By including the crosslinking aid in the above range, the degree of crosslinking of the composition for an encapsulant film can be maintained high, and the time required for impregnation of the ethylene / α-olefin copolymer with the crosslinking aid can be shortened.
[0054] (d) Silane coupling agent The composition for an encapsulant film of the present invention contains a silane coupling agent, which can improve the adhesive strength between the encapsulant film and the solar cell.
[0055] The silane coupling agent may be, for example, one or more selected from the group consisting of N-(β-aminoethyl)-γ-aminopropyltrimethoxysilane, N-(β-aminoethyl)-γ-aminopropylmethyldimethoxysilane, γ-aminopropyltriethoxysilane, γ-glycidoxypropyltrimethoxysilane, and γ-methacryloxypropyltrimethoxysilane (MEMO), but is not limited thereto.
[0056] The silane coupling agent may be included in an amount of 0.1 to 1.0 parts by weight, or 0.1 to 0.4 parts by weight, based on 100 parts by weight of the ethylene / α-olefin copolymer.
[0057] When the content of the silane coupling agent is within the above range, the adhesive strength with the glass during the fabrication of the solar cell module is excellent, and degradation of the long-term performance of the module due to moisture penetration can be prevented.
[0058] The composition for an encapsulant film of the present invention may further contain one or more selected from the group consisting of an unsaturated silane compound, an aminosilane compound, a light stabilizer, a UV absorber, and a heat stabilizer.
[0059] The unsaturated silane compound may be grafted to a main chain containing polymerized units of the monomer of the copolymer of the present invention in the presence of a radical initiator, etc., and may be included in a polymerized form in the silane-modified resin composition or the aminosilane-modified resin composition.
[0060] The unsaturated silane compound may be vinyltrimethoxysilane, vinyltriethoxysilane, vinyltrippropoxysilane, vinyltriisopropoxysilane, vinyltributoxysilane, vinyltripentoxysilane, vinyltriphenoxysilane, or vinyltriacetoxysilane, and examples thereof include, but are not limited to, vinyltrimethoxysilane or vinyltriethoxysilane.
[0061] Furthermore, the aminosilane compound acts as a catalyst to promote the hydrolysis reaction that converts reactive functional groups, such as alkoxy groups of unsaturated silane compounds grafted to the main chain of the copolymer during the graft modification step of the ethylene / α-olefin copolymer, into hydroxy groups, thereby further improving the adhesive strength with the upper and lower glass substrates or backsheets made of fluororesin, etc. In addition, the aminosilane compound directly participates in the copolymerization reaction as a reactant, thereby providing the aminosilane-modified resin composition with a moiety having an amine functional group.
[0062] The aminosilane compound is not particularly limited as long as it is a silane compound containing an amine group and is a primary amine or a secondary amine. For example, aminotrialkoxysilane, aminodialkoxysilane, etc. can be used as the aminosilane compound. Examples thereof include 3-aminopropyltrimethoxysilane (APTMS), 3-aminopropyltriethoxysilane (APTES), bis[(3-triethoxysilyl)propyl]amine, bis[(3-trimethoxysilyl)propyl]amine, 3-aminopropylmethyldiethoxysilane, 3-aminopropylmethyldimethoxysilane, N-[3-(trimethoxysilyl)propyl]ethylenediamine (DAS), aminoethylaminopropyltriethoxysilane, aminoethylaminopropylmethyldimethoxysilane, aminoethylaminopropylmethyldiethoxysilane, Examples of suitable aminosilane compounds include at least one selected from the group consisting of silane, aminoethylaminomethyltriethoxysilane, aminoethylaminomethylmethyldiethoxysilane, diethylenetriaminopropyltrimethoxysilane, diethylenetriaminopropyltriethoxysilane, diethylenetriaminopropylmethyldimethoxysilane, diethyleneaminomethylmethyldiethoxysilane, (N-phenylamino)methyltrimethoxysilane, (N-phenylamino)methyltriethoxysilane, (N-phenylamino)methylmethyldimethoxysilane, (N-phenylamino)methylmethyldiethoxysilane, 3-(N-phenylamino)propyltrimethoxysilane, 3-(N-phenylamino)propyltriethoxysilane, 3-(N-phenylamino)propylmethyldimethoxysilane, 3-(N-phenylamino)propylmethyldiethoxysilane, and N-(N-butyl)-3-aminopropyltrimethoxysilane. The aminosilane compounds may be used alone or in combination.
[0063] The light stabilizer may act to capture active species that initiate photodegradation of the resin and prevent photooxidation depending on the application of the composition. The type of light stabilizer that can be used is not particularly limited, and known compounds such as hindered amine compounds or hindered piperidine compounds can be used.
[0064] The UV absorber can absorb ultraviolet rays from sunlight or the like depending on the intended use of the composition, convert them into harmless thermal energy within the molecule, and prevent the excitation of active species that initiate photodegradation in the resin composition. The specific type of UV absorber that can be used is not particularly limited, and for example, one or a mixture of two or more inorganic UV absorbers such as benzophenone-based, benzotriazole-based, acrylonitrile-based, metal complex salt-based, hindered amine-based, ultrafine particle titanium oxide, or ultrafine particle zinc oxide can be used.
[0065] Examples of the heat stabilizer include phosphorus-based heat stabilizers such as tris(2,4-di-tert-butylphenyl)phosphite, bis[2,4-bis(1,1-dimethylethyl)-6-methylphenyl]ethyl ester phosphorous acid, tetrakis(2,4-di-tert-butylphenyl)[1,1-biphenyl]-4,4′-diylbisphosphonate, and bis(2,4-di-tert-butylphenyl)pentaerythritol diphosphite; and lactone-based heat stabilizers such as a reaction product of 8-hydroxy-5,7-di-tert-butyl-furan-2-one and o-xylene, and one or more of the above may be used.
[0066] The contents of the light stabilizer, UV absorber, and heat stabilizer are not particularly limited. That is, the contents of the additives can be appropriately selected in consideration of the use of the resin composition, the shape and density of the additive, etc., and can usually be appropriately adjusted within a range of 0.01 to 5 parts by weight based on 100 parts by weight of the total solid content of the composition for encapsulant film.
[0067] <Encapsulant film and solar cell module> The present invention also provides an encapsulant film comprising the encapsulant film composition.
[0068] The encapsulant film of the present invention can be produced by molding the composition for encapsulant films into a film or sheet. The molding method is not particularly limited, and the composition can be produced by, for example, forming the composition into a sheet or film by a conventional process such as a T-die process or extrusion. For example, the encapsulant film can be produced in situ using an apparatus in which the process for producing a modified resin composition using the composition for encapsulant films and the process for forming the film or sheet are connected to each other.
[0069] The thickness of the encapsulant film may be adjusted to about 10 to 2,000 μm or about 100 to 1,250 μm, taking into consideration the support efficiency and breakage risk of elements in an optoelectronic device, weight reduction of the device, workability, etc., and may vary depending on the specific application.
[0070] The present invention also provides a solar cell module including the encapsulant film. In the present invention, the solar cell module may have a configuration in which the encapsulant film of the present invention fills the gaps between solar cells arranged in series or parallel, a glass surface is placed on the surface exposed to sunlight, and the back surface is protected by a backsheet. However, the present invention is not limited thereto, and various types and shapes of solar cell modules manufactured using encapsulant films in the art are all applicable to the present invention.
[0071] The glass surface may be made of tempered glass to protect the solar cell from external impact and prevent breakage, and may be made of low-iron tempered glass having a low iron content to prevent reflection of sunlight and increase the transmittance of sunlight, but is not limited thereto.
[0072] The backsheet is a weather-resistant film that protects the back surface of the solar cell module from the outside, and examples thereof include, but are not limited to, a fluorine-based resin sheet, a metal plate or foil such as aluminum, a cyclic olefin-based resin sheet, a polycarbonate-based resin sheet, a poly(meth)acrylic-based resin sheet, a polyamide-based resin sheet, a polyester-based resin sheet, and a composite sheet obtained by laminating a weather-resistant film and a barrier film.
[0073] In addition, the solar cell module of the present invention can be produced by any method known in the art, without any limitations, except that it contains the above-mentioned encapsulant film.
[0074] The solar cell module of the present invention is manufactured using an encapsulant film with excellent volume resistivity, and the encapsulant film can prevent electrons in the solar cell module from moving and causing current to leak out, thereby significantly suppressing the PID (Potential Induced Degradation) phenomenon, in which insulation deteriorates, causing leakage current and resulting in a sudden drop in module output.
[0075] Example The present invention will be described in more detail below with reference to examples. However, the following examples are for illustrative purposes only and are not intended to limit the scope of the present invention.
[0076] Example 1 As the ethylene / α-olefin copolymer, LF675 (ethylene / 1-butene copolymer, density 0.877 g / cc, MI 14.0) manufactured by LG Chemical was used.
[0077] Ethylene / α-olefin copolymer pellet resin was charged with TBEC (t-butylperoxy 2-ethylhexyl carbonate) as a crosslinking agent, 2.5 g (0.5 phr) of DAHX (diallyl 1,4-cyclohexanedicarboxylate), a compound represented by the following chemical formula 1-1, as a crosslinking aid, and MEMO (3-(trimethoxysilyl)propyl methacrylate) as a silane coupling agent, and then impregnation was carried out.
[0078] A Haake mixer was used for the impregnation process. The torque value was monitored over time while stirring at 40 rpm at a temperature of 41.5°C, and the impregnation was completed when the torque value increased sharply. Before the crosslinker was absorbed into the ethylene / α-olefin copolymer, it acted as a lubricant, maintaining a low torque value. However, once the crosslinker was completely absorbed, the torque value increased. Therefore, the point at which the torque value suddenly increased was defined as the impregnation completion time.
[0079] Examples 2 to 5, Comparative Examples 1 to 8 The encapsulant film was produced in the same manner as in Example 1, except that the types and contents of the crosslinking agent and crosslinking aid were changed as shown in Table 1 below.
[0080] [Table 1] [ka]
[0081] [Table 2]
[0082] Experimental Example 1 (1) Impregnation completion time As described above in Example 1, the time when the torque value suddenly increased was taken as the time when the impregnation was completed, and the time from the start of stirring to the completion of impregnation was measured.
[0083] (2) Degree of crosslinking (%) The degree of crosslinking was evaluated based on the CPIA (China Photovoltaic Industry Association) standard and ASTM D 2765. The encapsulant film prepared above was cut into a 10 cm x 10 cm piece, and then vacuum laminated at 150°C for 20 minutes (5 minutes vacuum / 1 minute pressure / 14 minutes pressure), to obtain a crosslinked test piece.
[0084] The crosslinked test specimens were cut into 2mm x 2mm pieces, weighed at 0.5g each, and placed in a 200-mesh iron cage. They were then dissolved in refluxing xylene for 5 hours. The test specimens were then dried in a vacuum oven, and the weights before and after reflux were compared to determine the degree of crosslinking for each specimen.
[0085] [Table 3]
[0086] As shown in Table 3, it was confirmed that Examples 1 to 5 all had shorter impregnation completion times than Comparative Examples 1 to 5, which used TAIC, which does not correspond to the compound represented by Chemical Formula 1, as a crosslinking aid. The experimental results for evaluating the degree of crosslinking are as follows. Comparative Examples 3 to 5, which showed much longer impregnation completion times than Comparative Example 1, were excluded from the evaluation of the degree of crosslinking.
[0087] Comparative Examples 6 and 7, which used organic peroxide crosslinkers with one-hour half-life temperatures below 115°C, outside the 115-130°C range, showed lower degrees of crosslinking than the Examples. In particular, when compared to Example 1, which used the same type and amount of crosslinking coagent, it was clearly confirmed that the degree of crosslinking varied depending on the type of crosslinker. On the other hand, Comparative Example 8 was a case in which no organic peroxide crosslinker with a one-hour half-life temperature of 115-130°C was used, and it was confirmed that crosslinking did not proceed at all when only DAHX was used.
[0088] Experimental Example 2 (1) Volume resistance The volume resistivity of the crosslinked film (thickness: 0.6 mm) prepared for evaluating the degree of crosslinking was measured using a KEITHLEY 8009 RESISTIVITY TEST FIXTURE. The volume resistivity was measured at a voltage of 1000 V for 600 seconds, and the result was used.
[0089] [Table 4]
[0090] As shown in Table 4 above, the composition for an encapsulant film according to the present invention improved the degree of crosslinking while shortening the impregnation completion time. At the same time, in order to show a sufficient insulating effect for use as a composition for an encapsulant film, the volume resistivity must be at least 1.0×10 16 However, it was found that an excellent level of volume resistance was achieved in all of the examples.
Claims
1. The composition comprises an ethylene / α-olefin copolymer, an organic peroxide crosslinking agent, a crosslinking aid, and a silane coupling agent, The crosslinking coagent includes a compound represented by the following Chemical Formula 1: The organic peroxide crosslinking agent has a one-hour half-life temperature of 115 to 130°C. 【Chemical 1】 (In the above Chemical Formula 1, n is an integer from 2 to 6.
2. 2. The composition for a sealant film according to claim 1, wherein the organic peroxide crosslinking agent is at least one selected from the group consisting of t-butylperoxy 2-ethylhexyl carbonate, t-amylperoxy 2-ethylhexyl carbonate, 1,1-di(t-butylperoxy)-3,3,5-trimethylcyclohexane, 1,1-di(t-butylperoxy)-cyclohexane, 2,2-di(t-amylperoxy)-butane, 2,2-di(t-butylperoxy)-butane, n-butyl-4,4-di(t-butylperoxy)valerate, polyether poly(t-butylperoxycarbonate), t-amylperoxy 3,5,5-trimethylhexanoate, t-butylperoxyacetate, and t-butylperoxybenzoate.
3. 2. The composition for sealing material films according to claim 1, wherein the organic peroxide crosslinking agent is used in an amount of 0.1 to 3.0 parts by weight based on 100 parts by weight of the ethylene / α-olefin copolymer.
4. 2. The composition for sealing material films according to claim 1, wherein the crosslinking aid is used in an amount of 0.1 to 3.0 parts by weight based on 100 parts by weight of the ethylene / α-olefin copolymer.
5. 2. The composition for an encapsulant film according to claim 1, wherein the silane coupling agent is used in an amount of 0.1 to 1.0 parts by weight based on 100 parts by weight of the ethylene / α-olefin copolymer.
6. The composition for a sealing material film according to claim 1 , wherein the crosslinking aid further comprises an allyl group-containing compound.
7. 7. The composition for a sealing material film according to claim 6, wherein the allyl group-containing compound comprises at least one selected from the group consisting of triallyl isocyanurate, triallyl cyanurate, diallyl phthalate, diallyl fumarate, and diallyl maleate.
8. The composition for a sealing material film according to claim 6, wherein the molar ratio of the compound represented by Chemical Formula 1 to the allyl group-containing compound is 1:0.1 to 1:
10.
9. The composition for a sealant film according to claim 1, wherein the α-olefin comprises at least one selected from the group consisting of propylene, 1-butene, 1-pentene, 4-methyl-1-pentene, 1-hexene, 1-heptene, 1-octene, 1-decene, 1-undecene, 1-dodecene, 1-tetradecene, 1-hexadecene, and 1-eicosene.
10. The composition for sealing material films according to claim 1, wherein the α-olefin is contained in an amount of more than 0 to 99 mol % based on the ethylene / α-olefin copolymer.
11. A sealant film comprising the sealant film composition according to claim 1 .
12. A solar cell module comprising the encapsulant film of claim 11.
Citation Information
Patent Citations
Resin composition for solar cell sealing material, solar cell sealing material arranged by use thereof, and solar battery module
JP2015211189A